Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX gene
2015 ◽
Vol 28
(1-2)
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AbstractX-linked hypophosphatemic rickets (XLH) is the most common inherited form of rickets. XLH is caused by inactivating mutations in the
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2000 ◽
Vol 110
(3)
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pp. 694-698
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1999 ◽
Vol 277
(2)
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pp. C225-C232
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2016 ◽
Vol 64
(5)
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pp. 364
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2016 ◽
Vol 155
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pp. 63-66
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